EP3471760A1 - Nouvelles formulations immunogènes comprenant des adjuvants polymères d'acide polyacrylique linéaires ou ramifiés - Google Patents

Nouvelles formulations immunogènes comprenant des adjuvants polymères d'acide polyacrylique linéaires ou ramifiés

Info

Publication number
EP3471760A1
EP3471760A1 EP17736804.0A EP17736804A EP3471760A1 EP 3471760 A1 EP3471760 A1 EP 3471760A1 EP 17736804 A EP17736804 A EP 17736804A EP 3471760 A1 EP3471760 A1 EP 3471760A1
Authority
EP
European Patent Office
Prior art keywords
polyacrylic acid
acid polymer
antigen
salt
vaccine composition
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP17736804.0A
Other languages
German (de)
English (en)
Inventor
Guillaume Rigaut
Alexis Guy André Lucien PARISOT
Karelle DE LUCA
Christine Michele Pierrette Andreoni
Lydie REMOLUE
Marie GARINOT
Jean-Francois Cotte
Patricia PROBECK-QUELLECT
Jean Haensler
Véronique CHAMBON
Philippe Talaga
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Boehringer Ingelheim Vetmedica GmbH
Sanofi Pasteur Inc
Original Assignee
Sanofi Pasteur Inc
Merial Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sanofi Pasteur Inc, Merial Inc filed Critical Sanofi Pasteur Inc
Publication of EP3471760A1 publication Critical patent/EP3471760A1/fr
Pending legal-status Critical Current

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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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    • A61K39/0005—Vertebrate antigens
    • A61K39/0011—Cancer antigens
    • A—HUMAN NECESSITIES
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    • A61K39/12—Viral antigens
    • A61K39/145—Orthomyxoviridae, e.g. influenza virus
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    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
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    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/26—Carbohydrates, e.g. sugar alcohols, amino sugars, nucleic acids, mono-, di- or oligo-saccharides; Derivatives thereof, e.g. polysorbates, sorbitan fatty acid esters or glycyrrhizin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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    • A—HUMAN NECESSITIES
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    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A61P37/04—Immunostimulants
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F6/00—Post-polymerisation treatments
    • C08F6/001—Removal of residual monomers by physical means
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    • A61K2039/51—Medicinal preparations containing antigens or antibodies comprising whole cells, viruses or DNA/RNA
    • A61K2039/525—Virus
    • A61K2039/5254—Virus avirulent or attenuated
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    • A61K2039/525—Virus
    • A61K2039/5256—Virus expressing foreign proteins
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    • A61K2039/55—Medicinal preparations containing antigens or antibodies characterised by the host/recipient, e.g. newborn with maternal antibodies
    • A61K2039/552—Veterinary vaccine
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    • A—HUMAN NECESSITIES
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    • A61K2039/55516—Proteins; Peptides
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    • A61K2039/55522—Cytokines; Lymphokines; Interferons
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    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55555—Liposomes; Vesicles, e.g. nanoparticles; Spheres, e.g. nanospheres; Polymers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55561—CpG containing adjuvants; Oligonucleotide containing adjuvants
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/57—Medicinal preparations containing antigens or antibodies characterised by the type of response, e.g. Th1, Th2
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/58—Medicinal preparations containing antigens or antibodies raising an immune response against a target which is not the antigen used for immunisation
    • A61K2039/585—Medicinal preparations containing antigens or antibodies raising an immune response against a target which is not the antigen used for immunisation wherein the target is cancer
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00—Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F120/00—Homopolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride, ester, amide, imide or nitrile thereof
    • C08F120/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F120/04—Acids; Metal salts or ammonium salts thereof
    • C08F120/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Definitions

  • Novel immunogenic formulations comprising linear or branched polyacrylic acid polymer adjuvants
  • This invention belongs to the field of vaccines.
  • the invention is related to particular adjuvants and adjuvanted compositions and to processes for preparing such adjuvants and adjuvanted compositions.
  • polymers including acrylic acid units as an adjuvant in vaccine composition
  • polyacrylic acid polymers recommended as an adjuvant are cross-linked polymers.
  • US 3,790,665 and US 3,919,411 describe the use of an acrylic acid polymer cross-linked with a polyallyl saccharide, as an adjuvant.
  • Adjuvants corresponding to polymers of acrylic or methacrylic acid which are cross-linked, especially with polyalkenyl ethers of sugars or polyalcohols are also described in US 7,163,926.
  • Such kinds of polymers are sold under the name CARBOPOL®.
  • CARBOPOL 974P, 934P and 971P which are cross-linked polymers with high Mw (i.e. about 3 million for 974P, according to the data provided by the producer) is described in US 7,163,926, EP 1058558 and WO 2009/118523.
  • WO 2005/065712 proposes a complex that comprises a narrow molecular weight distribution polymer that includes units derived from an acrylic acid or a salt thereof, and a substance that has a pharmacological activity against a pathogenic organism or a cancer, or one or more antigens or immunogens.
  • the polymer may be a homopolymer or a copolymer of an acrylic acid or methacrylic acid or a salt thereof.
  • a molecular weight of 100000 or less is advocated.
  • EP0804234 discloses the use of a polymer partially consisting of acrylic acid units (constitutive repeating units anionic) and ester of acrylic acid units (constitutive hydrophobic repeating units) as a vaccine adjuvant in an aqueous solution.
  • a polyacrylic acid polymer CARBOPOL ® 907 is compared in these documents to its advocated homologous partially esterified polyacrylic acid polymers and provides a poorer immune response.
  • CARBOPOL ® 907 is a polyacrylic acid polymer that is not available today anymore and whose characteristics cannot be reliably determined. It belongs to the CARBOPOL family which is known as cross-linked polymers. This polymer has a weight average molecular weight Mw which is different from a document to another one: the publication of Vaccine, 1998 Vol. 16, No.
  • the disclosure provides formulations comprising a new class of polymers as a vaccine adjuvant.
  • this class of polymers has demonstrated safety and efficacy in adjuvanting formulations across a wide variety of antigens, for use in administration of a wide variety of animal species.
  • This class of polymers produces advantageous adjuvant properties, in comparison with other families of polyacrylic acid polymers used in the prior art.
  • the invention provides a family of polymers that is particularly effective as an adjuvant.
  • the invention provides a class of polymers that unexpectedly promotes strong Th-1 responses, in addition to Th-2 responses.
  • some polymers selected according to the invention lead to an adjuvant composition and, as a result to a vaccine composition.
  • the vaccine compositions of the instant disclosure are safer, particularly as to reproducibility and reduction of contaminants, which are often incompatible with vaccine storage stability.
  • the selected polymers are also stable and sterilizable by autoclaving.
  • the invention concerns a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer, for its use as an adjuvant in a vaccine composition, characterized in that said polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 350 to 650 kDa.
  • said polyacrylic acid polymer salt is exclusively composed of units corresponding to a salt of acrylic acid or is exclusively composed of units corresponding to the free acid form of acrylic acid and of units corresponding to a salt of acrylic acid.
  • said polyacrylic acid polymer salt comprises less than 0.005%, preferably less than 0.001%, w/w of oxidizing agents, based on the total dry weight of said polyacrylic acid polymer salt and/or comprises less than 0.005%, preferably less than 0.001%, w/w of persulfates, based on the total dry weight of said polyacrylic acid polymer salt.
  • said polyacrylic acid polymer is a salt with Na + .
  • said polyacrylic acid polymer salt has a polydispersity index below or equal to about 4, preferably below or equal to about 2.5.
  • said polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 4; or has a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 4; or has a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 2.5; or has a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 2.
  • said polyacrylic acid polymer salt comprises less than 0.005% w/w of acrylic acid monomer in free acid form or salt form, based on the total dry weight of said polyacrylic acid polymer salt.
  • said polyacrylic acid polymer salt is diafiltered and sterilized.
  • the polyacrylic acid polymer salt described in the invention is used for enhancing the Th1 immune response obtained with the vaccine composition.
  • the Th1 immune response is higher than the Th1 immune response obtained when polyacrylic acid polymer salt of lower molecular weight Mw are used, as adjuvant.
  • Another aspect of the invention also concerns a process for the preparation of a pharmaceutically acceptable salt of a polyacrylic acid polymer described in the invention comprising the following successive steps:
  • the invention also concerns a process for the storage of a solution of the polyacrylic acid polymer salt described in the invention comprising such a preparation process, followed by a storage step of the obtained pharmaceutically acceptable salt of the polyacrylic acid polymer, in solution.
  • the invention also concerns a vaccine composition
  • a vaccine composition comprising at least one vaccine agent (e.g. an immunogen or a nucleic acid encoding an immunogen) and a pharmaceutically acceptable salt of polyacrylic acid polymer described in the invention.
  • the immunogen may be selected from: inactivated pathogens, attenuated pathogens, sub-unit antigens, purified antigens, unpurified antigens, or antigens produced recombinantly using bacterial, yeast, plant, insect, or animal cells, expression vectors including plasmids, and the like.
  • the antigens may be purified by means well-known in the art including, but not limited to, ultrafiltration, ultracentrifugation, size-exclusion gel-filtration, ion-exchange chromatography, and PEG-purification.
  • the pathogen may be bacterial, viral, protozoal, or fungal in origin or the immunogen may constitute an antitoxin.
  • the present invention provides for a method of inducing an immune response in a vaccinate against a pathogen comprising administering the vaccine composition of the present invention to the vaccinate.
  • the term“about,” as used herein, means approximately, in the region of, roughly, or around. When the term“about” is used in conjunction with a numerical range, it modifies that range by extending the boundaries above and below the numerical values set forth. In general, the term“about” is used herein to modify a numerical value above and below the stated value by a variance of 10%. In one aspect, the term“about” means plus or minus 20% of the numerical value of the number with which it is being used. Therefore, about 50% means in the range of 45%-55%. Numerical ranges recited herein by endpoints include all numbers and fractions subsumed within that range (e.g. 1 to 5 includes 1, 1.5, 2, 2.75, 3, 3.90, 4, and 5). It is also to be understood that all numbers and fractions thereof are presumed to be modified by the term "about.”
  • FIG. 1 is a graph showing antibody titers (IgG1 and IgG2a) for OF1 mice immunized on D0, D21 and D35 with 2.5 ⁇ g PS5-rEPA per mouse per injection, injected alone or co-injected with either 200 ⁇ g CARBOPOL, PAA20 or PAA225000;
  • FIG. 2 is a is a graph showing the Geometric mean neutralizing antibody titer (GMT) of sera of groups of C57BL/6 mice immunized with 2 ⁇ g of hCMV-gB and squalene emulsion, PAA3000, PAA6000, PAA50000, PAA60000, PAA20 or PAA225000, as measured on MRC5 fibroblasts;
  • GCT Geometric mean neutralizing antibody titer
  • FIG. 3 is a graph showing the GMT for the groups of FIG. 2, as determined by seroneutralization on ARPE-19 cells (human epithelial cells);
  • FIG. 4 is a graph showing serum IgG1 antibodies directed against hCMV-gB antigen for the groups of FIG.2, as determined by ELISA;
  • FIG. 5 is a graph showing serum IgG2c antibodies directed against hCMV-gB antigen for the groups of FIG.2, as determined by ELISA;
  • FIG.6 is a graph showing IL5 cytokine levels for the groups of FIG.2, as measured using the CBA Flex set Kit;
  • FIG. 7 is a graph showing IFN ⁇ cytokine levels for the groups of FIG. 2, as measured using the CBA Flex set Kit;
  • FIG. 8 is a graph presenting the rabies serology for canine groups vaccinated with inactivated rabies + PAA225000; AF03; PAA60000; or Squalene Emulsion
  • FIG. 9 is a graph presenting the CIV serology for canine groups vaccinated with canarypox-vectored recombinant influenza + (1) PBS; (2) CARBOMER (4 mg/ml); (3) PAA60000 (4mg/ml); or (4) PAA225000 (4mg/ml).
  • Group 5 received only PBS (i.e. neither recombinant flu antigen nor adjuvant);
  • FIG.10 is a graph presenting an expansion of the Day 41 serology data shown in FIG.9;
  • FIG. 11 is a graph showing the mean SRH-determined influenza antibody titer for equine groups vaccinated with vCP1533+vCP2242 (each harboring an HA gene from influenza virus) & tetanus toxin one of the following: (A) CARBOMER (4 mg/mL); (B) PAA60000 (4 mg/mL); (C) PAA225000 (4 mg/mL); (D) ADVAX1 (20 mg/mL); (E) ADVAX2 (20 mg/mL). Group (F) received only PBS (i.e. neither antigen nor adjuvant);
  • FIG. 12 is a graph showing the tetanus serology for each equine group to D35. Groups: same as depicted in FIG.11;
  • FIG.13 is a graph showing the equine tetanus serology results out to D63;
  • FIG. 14 is a graph showing the mean SpaA serology for each porcine group (to D59).
  • Groups (G1) SpaA + TS6; (G2) SpaA + PAA60000; (G3) SpaA + PAA225000; SpaA–FlaB-His + PBS; (G5) SpaA–FlaB-His + PAA225000; (G6) PBS.
  • polyacrylic acid polymer we mean a polymer which is exclusively composed of acrylic acid units. So, in the form of a salt, said polyacrylic acid polymer salt is exclusively composed of units corresponding to a salt of acrylic acid or is exclusively composed of units corresponding to the free acid form of acrylic acid and of units corresponding to a salt of acrylic acid.
  • a linear or a branched polyacrylic acid polymer is obtained by polymerization of only acrylic acid as monomer.
  • the polymerization is, most of the time, carried out by radical polymerization, using an oxidizing agent as initiator or catalyst.
  • the most used oxidizing agents are persulfate (peroxydisulfate), for instance sodium or potassium persulfate.
  • Branched polyacrylic acid polymers are, for instance, described in Macromolecules 2011, 44, 5928–5936.
  • the polymer according to the invention is linear, its Mark Houwink slope is higher or equal to 0.7 (Yan J.K., Pei J.J., Ma H.L., Wang Z.B. 2015. Effects of ultrasound on molecular properties, structure, chain conformation and degradation kinetics of carboxylic curdlan. Carb. Polymers.121, 64-70).
  • salt of the polyacrylic acid polymer we mean salt of anionic forms of the polymer with cation(s), in particular with monovalent cation(s), which is(are) pharmaceutically acceptable.
  • monovalent cation are alkali metal cations, such as Na + or K + , or ammonium cations such as NH +
  • the acidic groups of the polyacrylic acid polymer will be in an anionic form, forming a salt with a cation which will also be present in the aqueous solution.
  • the acid groups of the polymer may be exclusively in the free acid form or, in salt cases, the acid groups of the polymer may be exclusively in the salt form, or some acid groups may be in the acidic form and others in the salt form.
  • the preferred salts of the polyacrylic acid polymers of the invention are salts with Na + .
  • the polyacrylic acid polymer will preferably be in the form of a sodium salt and, in that case, all the characteristics (Mw, IP, monomer and persulfate contents...) will concern the salt (i.e. the sodium salt) of the polyacrylic acid polymer.
  • this“pharmaceutically acceptable salt of polyacrylic acid polymer” will simply be called the“polyacrylic acid polymer salt” and is preferably a polyacrylic acid polymer sodium salt.
  • the polyacrylic acid polymer salt can be in a solid form (precipitate or powder) or preferably in a liquid formulation.
  • a liquid formulation will include the polyacrylic acid polymer salt and an aqueous solution.
  • a formulation has a pH in the range of 5.5 to 8.0. This pH can be obtained by incorporation of a base, like NaOH, in the aqueous solution.
  • the aqueous solution can be a buffered aqueous solution, obtained with a buffer such as a phosphate buffer, a TRIS (2-amino-2-hydroxymethyl-1,3-propanediol), Hepes (acide 4-(2-hydroxyethyl)-1- piperazine ethane sulfonique), histidine or citrate buffer.
  • a buffer such as a phosphate buffer, a TRIS (2-amino-2-hydroxymethyl-1,3-propanediol), Hepes (acide 4-(2-hydroxyethyl)-1- piperazine ethane sulfonique), histidine or citrate buffer.
  • the liquid formulation may also comprise one or several additional salts, such as NaCl.
  • a polyacrylic acid polymer salt or a liquid formulation of a polyacrylic acid polymer salt having one of the following characteristics, any combination of such characteristics or even all the following characteristics if they do not exclude one another:
  • the polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 350 to 650 kDa;
  • the polyacrylic acid polymer salt or the liquid formulation of the polyacrylic acid polymer salt comprises less than 0.005%, preferably less than 0.001%, w/w of oxidizing agents, based on the total dry weight of said polyacrylic acid polymer salt and/or less than 0.005%, preferably less than 0.001% , w/w of persulfates, based on the total dry weight of said polyacrylic acid polymer salt;
  • the polyacrylic acid polymer salt has a polydispersity index below or equal to 4, preferably below or equal to 2.5;
  • the polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 4 or has a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 4;
  • the polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 2.5 or has a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 2;
  • the polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7;
  • the polyacrylic acid polymer salt or the liquid formulation of the polyacrylic acid polymer salt comprises less than 0.005% w/w of acrylic acid monomer in free acid form or salt form, based on the total dry weight of said polyacrylic acid polymer salt.
  • this polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7, or
  • this polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7, or
  • this polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7, or
  • this polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7.
  • the polyacrylic acid polymer salt under the liquid formulation is diafiltered.
  • the polyacrylic acid polymer salt or the liquid formulation of the polyacrylic acid polymer salt is sterilized.
  • the polyacrylic acid polymer salt or the liquid formulation of the polyacrylic acid polymer salt is diafiltered, the sterilization occurs after the diafiltration.
  • the weight average molecular weight Mw is obtained by size exclusion chromatography.
  • three detectors will be used after the size exclusion chromatography column: a right angle light scattering detector, a refractive index detector and a four-capillary differential viscometer.
  • the detailed procedures which are provided in the examples are preferably used according to the invention for the determination of the Mw, IP (polydispersity index), polymer concentration and Mark Houwink slope.
  • the dn/dc used for the determination of Mw is preferably determined using the refractive index detector with a panel of polyacrylic acid polymers of known concentration.
  • the content of persulfate and the content of acrylic acid monomer in free acid form or salt form can be determined by High Performance Anion Exchange Chromatography with conductimetric detection.
  • the protocol which is detailed in the examples, in particular in paragraph B of“I.2 Determination of persulfates and acrylate monomers” may be used.
  • polyacrylic acid polymer raw material there is residual monomer content which corresponds to acrylic acid or acrylate salt content which did not polymerize.
  • an initiator of polymerization most of the time an oxidizing agent such as persulfates, is used as a catalyst to initiate the polymerization.
  • an oxidizing agent such as persulfates
  • polyacrylic acid polymer raw material there may remain a residual content of initiator of polymerization (most of the time, oxidizing agent such as persulfate) which has not been consumed by the polymerization process.
  • Polyacrylic acid polymers on the markets are often lacking specifications about residual monomer, and oxidizing agent(s) contents and about their precise Mw and their oligomer content.
  • the invention concerns a process for the preparation of a pharmaceutically acceptable salt of polyacrylic acid polymer, in particular of the pharmaceutically acceptable salt of polyacrylic acid polymer as defined in the paragraph“Features of the polyacrylic acid polymer” comprising the following successive steps:
  • the solution can be a solution of the polyacrylic acid polymer directly in the form of the desired pharmaceutically acceptable salt, or at least partly, in the form of its free acid form. If in step a), the solution is a solution of the polyacrylic acid polymer in its free acid form, a salification can be carried out after the purification of step b) and the sterilization of step c) performed on the solution of the desired pharmaceutically acceptable salt. It is also possible to carry out the sterilization of step c) on the solution of the polyacrylic acid polymer in its free acid form and to perform a salification after sterilization.
  • a salification is required, it may be obtained by the introduction of a base, like NaOH or KOH in the solution, depending on the desired salt.
  • the purification and/or the sterilization are carried out on a solution of a pharmaceutically acceptable salt of the polyacrylic acid polymer.
  • This solution is, for instance, a buffered aqueous solution, in particular with a phosphate buffer or with a TRIS, Hepes, histidine or citrate buffer.
  • the aqueous solution of the pharmaceutically acceptable salt of the polyacrylic acid polymer may also comprise one or several additional salts, such as NaCl.
  • the process according to the invention for the preparation of a pharmaceutically acceptable salt of polyacrylic acid polymer, in particular of the pharmaceutically acceptable salt of polyacrylic acid polymer as defined in the paragraph“Features of the polyacrylic acid polymer”, comprises the following successive steps:
  • the polyacrylic acid polymer of the solution of step a) has a Mark Houwink slope higher or equal to 0.7.
  • this Mark Houwink slope concerns the polyacrylic acid polymer salt.
  • the purification will remove small molecules.
  • the purification may be performed by dialysis, diafiltration, ultrafiltration or size exclusion chromatography. Diafiltration and ultrafiltration use cross-flow filtration (also called tangential flow filtration) on a porous membrane.
  • a solution containing the polyacrylic acid polymer circulates on the membrane: a part of the solution including the small molecules is eliminated in the permeate which will pass through the membrane.
  • Another part of the solution, called the retentate, including the purified polyacrylic polymer will circulate on the surface of the membrane.
  • the retentate can circulate in a circulation loop and be diafiltered or ultrafiltered several times.
  • Solvent typically aqueous buffer or saline aqueous solution
  • Solvent is added to the retentate which circulates, to replace the permeate volume, at the same rate as the permeate flow rate, such that the volume of the retentate remains constant.
  • the size of the eliminated molecules is determined by the cut-off of the membrane.
  • membranes with a cut-off from 1 to 80 kDa, preferably from 2 to 50 kDa may be used. Such membranes are for instance available at Merck Millipore.
  • the cut-off of a membrane is rated according to its Nominal Molecular Weight Limit (NMWL) or its Molecular Weight Cut Off (MWCO).
  • a UF membrane rated at 30 kD will exclude a test protein with a molecular weight of 30 kiloDaltons. Ninety percent of that test protein will remain in the retentate and 10% will pass through into the permeate, resulting in concentration of the protein if no buffer or saline solution is added to the retentate during the process.
  • the flow of retentate circulation is from 50 to 80 L/H/m 2 .
  • the Transmembrane Pressure (TMP) is, for instance, at 0.9 +/- 0.1 bar.
  • the purification in step b) may be carried out by dialysis, diafiltration, ultrafiltration or size exclusion chromatography.
  • the purification may be performed on a solution containing from 2 to 50 mg/ml, preferably, from 10 to 30 mg/ml of the polyacrylic acid polymer.
  • this concentration concerns the polymer salt.
  • the purification is carried out by diafiltration with a membrane having a cut-off from 1 to 80 kDa, preferably from 2 to 50 kDa.
  • the purification is carried out in conditions allowing the recovery of a polyacrylic acid polymer in solution having:
  • the weight average molecular weight Mw of the recovered polyacrylic acid polymer may be in the range of 350 to 650 kDa and its polydispersity index below or equal to 4.
  • the purification device will be chosen in order to eliminate the desired impurities. For instance, when ultrafiltration or diafiltration is used for purification, the cut-off of the membrane will be chosen, depending on the impurities to eliminate. With a cut-off of at least 20 kDa, essentially, the small molecules like persulfates and monomers are eliminated by cross-filtration. With a cut-off higher than 20 kDa, bigger molecules like oligomers are also eliminated and, as a result, the purification leads to a decrease of the IP and to an increase of the Mw.
  • the diafiltration or ultrafiltration is carried out with a cut-off for the membrane used, or more generally the purification is carried out in conditions, allowing the recovery of a polyacrylic acid polymer in solution having: a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 2.5 ; or a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 2, and
  • the solution obtained after the purification steps contains from 2 to 50 mg/mL of the polyacrylic acid polymer salt, in particular at least 10 mg/ml of the polyacrylic acid polymer salt.
  • the main result of the purifying process is the elimination of small molecules, such as oxidizing agent (i.e. persulfate) and acrylate monomers.
  • oxidizing agent i.e. persulfate
  • acrylate monomers By systematically carrying out such a purifying step, the characteristics of the polymer composition that is used as an adjuvant can be better defined and the composition is safer and more stable.
  • the content of acrylic acid monomer which is suspected of being embryotoxic and teratogenic, is considerably reduced.
  • the sterilization may be performed by sterilizing filtration(s) or preferably, by autoclaving. Sterilizing filtration is performed on a 0.2 ⁇ m pore membrane. The elimination of the oxidizing agent allows the use of sterilization by autoclaving which is recommended by Pharmacopeias.
  • the autoclaving can be performed at a temperature from 100 to 150°C, and during a time from 5 minutes to one hour. With the purifying step, the obtained polymer is more stable in time and more resistant to heat treatment.
  • the invention also concerns a process for the storage of a solution of a pharmaceutically acceptable salt of polyacrylic acid polymer, in particular of the pharmaceutically acceptable salt of polyacrylic acid polymer as defined in the paragraph“Features of the polyacrylic acid polymer”, comprising the preparation process as defined according to the invention, followed by a storage step of the obtained pharmaceutically acceptable salt of the polyacrylic acid polymer, in solution.
  • the storage step may last from 1 day to 2 years.
  • the temperature of storage will be, most of the time, in the range of 0 to 30 °C, in particular at 2-8°C or at room temperature, generally around 22°C.
  • the storage can be performed directly after the step c) of sterilizing.
  • Such a storage of the adjuvant in a liquid form is very advantageous and avoids additional manipulations, by comparison to a storage in dry form which necessitates polymer resuspension/dilution for the preparation of the vaccine composition.
  • the liquid solution of the polyacrylic acid polymer salt comprises less than 0.005%, preferably less than 0.001% w/w of oxidizing agents, based on the total dry weight of said polyacrylic acid polymer salt and/or less than 0.005%, preferably less than 0.001% w/w of persulfates, based on the total dry weight of said polyacrylic acid polymer salt, the solution is particularly stable.
  • the storage step is carried out by placing the solution of the polyacrylic acid polymer salt in a container and storing it.
  • the stored solution for instance, contains from 2 to 50 mg/mL of the polyacrylic acid polymer salt.
  • a dilution or a concentration step can be carried out for obtaining the desired concentration, for instance after step b) of the preparation process.
  • the polyacrylic acid polymer salt may be, for instance, in an aqueous solution or in a buffered aqueous solution.
  • the pH of the stored solution is usually between 5.5 and 8, and more preferably between 6.5 and 7.5 (e.g. about 7). Stable pH may be maintained by the use of a buffer e.g. a Tris buffer, a citrate buffer, phosphate buffer, a Hepes buffer, or a histidine buffer.
  • the aqueous solution may also comprise one or several additional salts, such as NaCl.
  • the storage can be performed by keeping the solution of the polyacrylic acid polymer salt away from light. For that, a dark or opaque container can be used.
  • the invention also concerns the polyacrylic acid polymer salt, as defined in the invention, whatever the described embodiment in relation with the above paragraph“Features of the polyacrylic acid polymer” for its use as an adjuvant in a vaccine composition or for its use as an adjuvant to a vaccine agent in raising an immune response in an individual, in particular in a human being.
  • An adjuvant composition for vaccine comprising an aqueous solution of a pharmaceutically acceptable salt of polyacrylic acid polymer, as defined in the invention, whatever the described embodiment in relation with the above paragraph“Features of the polyacrylic acid polymer” is also an object of the invention.
  • Adjuvant refers to a compound that modulates the immunogenicity of a vaccine composition.
  • a vaccine composition classically includes a vaccine agent which can be an antigen or a vector (live recombinant viral vector or nucleic acid) encoding an antigen. More precisely, an adjuvant modulates the immunogenicity of the antigen present or encoded by the nucleic acid present in the composition.“Modulate the immunogenicity” includes enhancing the magnitude and/or duration of an immune response induced by the antigen, and includes in particular the enhancement of the antibody response (especially virus neutralizing antibodies or bactericidal antibodies) and/or the enhancement of the cellular immune responses (enhancement of CD4+ and/or CD8+ T cell responses).
  • the polymer selected according to the invention has different advantages, as shown by the examples. For instance, in comparison with analogous linear or ramified polymers of lower Mw, they lead to increased immune responses.
  • CD4+ lymphocytes also called "helper" T cells
  • helper T cells are immune response mediators.
  • two types of effector CD4+ T helper cell responses are characterized by cytokine profiling and antibody subtyping.
  • the use of the polyacrylic acid polymer, as defined in the invention has the advantage to promote strong Th-1 responses (results on IFN- ⁇ , TNF- ⁇ and IgG2a antibodies in mice were obtained) in addition to the Th-2 responses (results on Il-4, IL-5 and IgG1 antibodies in mice were obtained) that are commonly induced by human adjuvants of the prior art (aluminum salts, oil-in-water emulsions).
  • Th-1 immunity is important to fight viral and intracellular bacterial infections, as well as cancer, since Th-1 immune responses support the activation of macrophages and of other killer cells (e.g. CD8+ T lymphocytes or Cytotoxic T Lymphocytes) to kill intracellular pathogens, infected cells and tumor cells.
  • macrophages e.g. CD8+ T lymphocytes or Cytotoxic T Lymphocytes
  • the polyacrylic acid polymer salt of the invention and the vaccine agent can be formulated in a same composition, in particular in an aqueous composition, or in two different compositions and mixed just before administration.
  • the vaccine composition can include two vials: one contains the vaccine agent and the other contains the polyacrylic acid polymer salt.
  • the polyacrylic acid polymer salt in a liquid formulation is contained in a first vial and the vaccine agent in a freeze-dried or lyophilized form, in particular the selected antigen in a freeze-dried or lyophilized form, is contained in a second vial.
  • the formulation of the polyacrylic acid polymer salt will be used for rehydrating the vaccine agent, in particular the selected antigen.
  • the invention also concerns the polyacrylic acid polymer salt, as defined in the invention, whatever the described embodiment in relation with the above paragraph“Features of the polyacrylic acid polymer” for its use as an adjuvant in a vaccine composition which enhances the obtained Th1 immune response and/or which balances the obtained Th1 and Th2 immune responses.
  • the polyacrylic acid polymer salt, as defined in the invention is used as an adjuvant to a vaccine agent for raising the immune response in an individual, in particular in a human being, and enhancing the obtained Th1 immune response and/or balancing the obtained Th1 and Th2 immune responses.
  • the vaccine composition according the invention may comprise any vaccine agent that can be used in a vaccine, such as an antigen or a vector (live viral vector or nucleic acid, including DNA and RNA) encoding an antigen.
  • a vaccine such as an antigen or a vector (live viral vector or nucleic acid, including DNA and RNA) encoding an antigen.
  • the term "antigen" is intended to mean any molecule containing one or more epitopes (either linear, conformational or both), that elicits an immunological response.
  • the antigen(s) which can be used in a vaccine composition according to the invention can be a living, attenuated, killed, inactivated or non-infectious whole microorganism, an extract or split of a microorganism, a subunit form of a natural antigen, a recombinant form or a hybrid form. When it is a subunit form, the nature of the antigen is of little importance.
  • the antigen may be a peptide, a protein, a glycoprotein, a polysaccharide, a glycolipid, a lipoprotein, a lipopeptide, a VLP (virus-like particle) ... etc.
  • the vaccine agent present in the composition is an antigen or a vector (recombinant virus or nucleic acid) encoding an antigen used or suitable to be used for the treatment or prevention of various diseases that may affect humans or animals other than humans, notably including: diphtheria, tetanus , polio, rabies, whooping cough, hepatitis A, hepatitis B, hepatitis C, yellow fever, typhoid fever, chickenpox, measles, mumps, rubella, Japanese encephalitis, influenza, meningitis, cholera, infections caused by Rotavirus, Norovirus, Rhinovirus, Respiratory Syncytial Virus, Herpes Simplex Virus, Papilloma Virus, cytomegalovirus virus, West Nile Virus, Dengue Virus, Chykungunya Virus, HIV (AIDS), bacterial diseases caused by streptococci, Chlamydia trachomatis and pneumoniae
  • the antigens can be of bacterial, viral or parasitic nature.
  • the bacterial antigens originated from Clostridium tetani, Clostridium diphtheriae, Bordetella pertussis, Haemophilus influenzae type B, Streptococcus pneumoniae, Neisseria meningitidis, Shigella sp, Salmonella typhi, Staphylococcus aureus or Staphylococcus epidermidis, Mycobacterium tuberculosis, Chlamydia trachomatis and pneumoniae or Streptococcus sp, the viral antigens originated from the hepatitis A, B or C virus, the influenza virus, the rhinovirus, the respiratory syncytial virus, the West Nile virus, the rabies virus, the poliovirus, the HIV virus, the dengue virus, the Japanese encephalitis virus, the yellow fever virus, the cytome
  • the vaccine agent present in the composition is an antigen or a vector (recombinant virus or nucleic acid) encoding an antigen originated from Staphylococcus aureus, or from the cytomegalovirus.
  • the vaccine composition of the invention may be a composition intended for immunization against a single pathogen or cancer, that is to say it comprises one or more vaccine agents, in particular one or more antigens, of a single pathogen or cancer, or may be a composition intended for immunization against several pathogens or cancers.
  • the vaccine composition according to the invention may also include one or several specific vaccine agents, in particular one or several antigens of a single disease, but which belong to different categories of this disease (multiple serotypes or strains, or clades, depending on the nature of the agent).
  • the polyacrylic acid polymer salt of the invention and the vaccine agent can be formulated in a composition with any pharmaceutically acceptable vehicle.
  • the expression“pharmaceutically acceptable vehicle” refers to a vehicle that is physiologically acceptable for administration to a mammal, and in particular to a human being, while retaining the physiological activity of the composition according to the invention, i.e. its ability to induce an immune response.
  • One exemplary pharmaceutically acceptable vehicle is a physiological saline buffer.
  • Other physiologically acceptable vehicles are known to those skilled in the art and are described, for instance, in Remington’s Pharmaceutical Sciences (18 th edition), ed. A. Gennaro, 1990, Mack Publishing Company, Easton, Pa.
  • the pH of the composition is usually between 5.5 and 8, and more preferably between 6.5 and 7.5 (e.g. about 7). Stable pH may be maintained by the use of a buffer e.g. a Tris buffer, a citrate buffer, phosphate buffer, a Hepes buffer, or a histidine buffer.
  • a buffer e.g. a Tris buffer, a citrate buffer, phosphate buffer, a Hepes buffer, or a histidine buffer.
  • the composition generally includes a buffer.
  • the composition may be sterile and/or pyrogen-free. Compositions may be isotonic with respect to humans.
  • composition may also comprise one or several additional salts, such as NaCl.
  • a composition according to the invention comprises an immunologically effective amount of the vaccine agent.
  • An“immunologically effective amount” is an amount which, when administered to a subject, is effective for eliciting an immune response against the antigen used or generated upon vector and/or nucleic acid expression. This amount can vary depending on the health and physical condition of the subject to be treated, their age, the capacity of the subject's immune system to produce antibodies, the degree of protection desired, the formulation of the vaccine, the treating doctor's assessment of the medical situation.
  • the vaccine composition according to the invention may also comprise allergen(s), in particular allergen(s) for desensitization in the treatment of allergies.
  • the vaccine composition according to the invention may be administered by any route commonly used for administering a vaccine.
  • a regimen leading to the induction of the expected immune response will be used.
  • the immunization schedule includes several administrations.
  • the amount of the composition administered is enough to produce the desired immune response.
  • the vaccine composition is in a liquid form considering the good stability properties of the polyacrylic acid polymer allowing the use of liquid forms which are less expensive to produce.
  • the parenteral injections are also preferred.
  • the polyacrylic acid polymer does not cause local apparent side effects after an intradermal injection. This can be an advantage over most other adjuvants (including aluminum salts) that are sometimes reactogenic through intradermal route.
  • a vaccine composition according to the invention comprises at least one vaccine agent and a pharmaceutically acceptable salt of polyacrylic acid polymer, said polyacrylic acid polymer salt having a weight average molecular weight Mw in the range of 350 to 650 kDa.
  • the vaccine composition according to the invention comprises per dose from 0.1 to 8 mg of the pharmaceutically acceptable salt of the polyacrylic acid polymer, preferably from 0.1 to 4 mg, and more preferably from 0.1 to 2 mg.
  • At least one vaccine agent is an antigen or a vector (viral vector or nucleic acid) encoding an antigen, the said antigen being a bacterial antigen originated from Clostridium tetani, Clostridium diphtheriae, Bordetella pertussis, Haemophilus influenzae type B, Streptococcus pneumoniae, Neisseria meningitidis, Shigella sp, Salmonella typhi, Staphylococcus aureus or Staphylococcus epidermidis, Mycobacterium tuberculosis, Chlamydia trachomatis or pneumoniae or Streptococcus sp ; a viral antigen originated from the hepatitis A, B or C virus, the influenza virus, the rhinovirus, the respiratory syncytial virus, the West Nile virus, the rabies virus, the poliovirus, the HIV virus, the dengue virus, the Japanese encephalitis virus, the yellow fever virus,
  • the vaccine agent present in the composition is an antigen or a vector (recombinant virus or nucleic acid) encoding an antigen originated from Staphylococcus aureus, or from the cytomegalovirus.
  • the vaccine compositions according to the invention are in a liquid form having a pH in the range of 5.5 to 8.0.
  • they include a phosphate buffer or a TRIS, Hepes, histidine or citrate buffer.
  • the polyacrylic acid polymer salt present in the vaccine composition has one of the following characteristics, any combination of such characteristics or even all the following characteristics if they do not exclude one another:
  • the polyacrylic acid polymer salt or the liquid formulation of the polyacrylic acid polymer salt comprises less than 0.005%, preferably less than 0.001% w/w of oxidizing agents, based on the total dry weight of said polyacrylic acid polymer salt and/or less than 0.005%, preferably less than 0.001% w/w of persulfates, based on the total dry weight of said polyacrylic acid polymer salt;
  • the polyacrylic acid polymer salt has a polydispersity index below or equal to 4, preferably below or equal to 2.5;
  • the polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 4 or has a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 4;
  • the polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 2.5 or has a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 2;
  • the polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7;
  • the polyacrylic acid polymer salt or the liquid formulation of the polyacrylic acid polymer salt comprises less than 0.005% w/w of acrylic acid monomer in free acid form or salt form, based on the total dry weight of said polyacrylic acid polymer salt,
  • the pharmaceutically acceptable salt of the linear or branched polyacrylic acid polymer is diafiltered and/or is sterilized.
  • polyacrylic acid polymer salt present in the vaccine composition is characterized by:
  • this polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7, or
  • this polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7, or
  • this polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7, or
  • this polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7.
  • the invention also relates to the vaccine compositions of the invention for their use in raising an immune response in an individual, in particular in a human being.
  • the subject matter of the invention also encompasses a method of raising an immune response in an individual, in particular, in a human being, comprising the step of administering to the individual in need thereof an immunologically effective amount of the composition according to the invention.
  • the individual can be a human being or an animal selected from a canine, a feline, a bovine, a porcine, an equine or an ovine species as well as the mustelids and the avian species.
  • the invention also relates to the vaccine compositions of the invention for their use in raising an immune response in an individual, in particular in a human being, with enhancement of the obtained Th1 immune response
  • the subject matter of the invention also encompasses a method of raising an immune response in an individual, in particular, in a human being, with enhancement of the obtained Th1 immune response, said method comprising the step of administering to the individual in need thereof an immunologically effective amount of the composition according to the invention.
  • the polyacrylic acid polymer or the polyacrylic acid polymer salt has been subjected to a purification, such as diafiltration, prior to its addition into the vaccine composition. More precisely, the polyacrylic acid polymer or the polyacrylic acid polymer salt has been subjected to a purification, such as diafiltration, followed by a sterilization, prior to its introduction into the vaccine composition.
  • the sterilization may be performed by sterilizing filtration(s) or, preferably, by autoclaving.
  • the vaccine composition can be prepared by simply mixing the polyacrylic acid polymer salt, in particular in a liquid form in an aqueous solution or in a buffered aqueous solution, and a suspension of the vaccine agent(s) and other component(s) that can be present in the composition. This can be done by adding one or more selected vaccine agents on the polyacrylic acid polymer salt, in particular on the polyacrylic acid polymer salt in a liquid formulation in an aqueous solution or in a buffered aqueous solution, or by adding the polyacrylic acid polymer, in particular the polyacrylic acid polymer in a liquid formulation in an aqueous solution or in a buffered aqueous solution, on a suspension already comprising the selected vaccine agent(s). On the other hand, in the case where it is desired to formulate vaccine compositions comprising multiple vaccine agents, it may be preferred to perform firstly the mixing of the polyacrylic acid polymer salt with one or more vaccine agent(s), and to incorporate the other(s) after.
  • the vaccine composition can be obtained by rehydration of the lyophilized agent(s) directly with the formulation (aqueous solution or buffered aqueous solution) containing the polyacrylic acid polymer salt.
  • the invention also concerns the use of the polyacrylic acid polymer salt, as defined in the invention, whatever the described embodiment in relation with the above paragraph“Features of the polyacrylic acid polymer”, in the preparation of a vaccine composition comprising at least one vaccine agent.
  • a process of a vaccine composition implementing the mixing of the polyacrylic acid polymer salt, as defined in the invention, whatever the described embodiment in relation with the above paragraph“Features of the polyacrylic acid polymer”, with at least one vaccine agent, is also an object of the invention.
  • the term“animal” includes all vertebrate animals including humans. It also includes an individual animal in all stages of development, including embryonic and fetal stages.
  • the term“vertebrate animal” includes, but not limited to, humans, canines (e.g., dogs), felines (e.g., cats); equines (e.g., horses), bovines (e.g., cow, cattle), porcine (e.g., pigs), as well as in avians.
  • the term“cow” or“cattle” is used generally to refer to an animal of bovine origin of any age.
  • Interchangeable terms include“bovine”,“calf”,“steer”,“bull”, “heifer”,“cow” and the like.
  • Interchangeable terms include“piglet”,“sow” and the like.
  • the term “avian” as used herein refers to any species or subspecies of the taxonomic class ava, such as, but not limited to, chickens (breeders, broilers and layers), turkeys, ducks, a goose, a quail, pheasants, parrots, finches, hawks, crows and ratites including ostrich, emu and cassowary.
  • the term“pig” or “piglet” means an animal of porcine origin, while“sow” refers to a female of reproductive age and capability.
  • the term“virulent” means an isolate that retains its ability to be infectious in an animal host.
  • the term“inactivated vaccine” means a vaccine composition containing an infectious organism or pathogen that is no longer capable of replication or growth.
  • the pathogen may be bacterial, viral, protozoal or fungal in origin. Inactivation may be accomplished by a variety of methods including freeze-thawing, chemical treatment (for example, treatment with formalin), sonication, radiation, heat or any other convention means sufficient to prevent replication or growth of the organism while maintaining its immunogenicity.
  • the term“immunogenicity” means capable of producing an immune response in a host animal against an antigen or antigens. This immune response forms the basis of the protective immunity elicited by a vaccine against a specific infectious organism.
  • immune response refers to a response elicited in an animal.
  • An immune response may refer to cellular immunity (CMI); humoral immunity or may involve both.
  • CMI cellular immunity
  • humoral immunity or may involve both.
  • the present invention also contemplates a response limited to a part of the immune system.
  • a vaccine composition of the present invention may specifically induce an increased gamma interferon response.
  • the term“antigen” or“immunogen” means a substance that induces a specific immune response in a host animal.
  • the antigen may comprise a whole organism, killed, attenuated or live; a subunit or portion of an organism; a recombinant vector containing an insert with immunogenic properties; a piece or fragment of DNA capable of inducing an immune response upon presentation to a host animal; a protein, a polypeptide, a peptide, an epitope, a hapten, toxin, antitoxin; or any combination thereof.
  • multivalent means a vaccine containing more than one antigen whether from the same species (i.e., different isolates of FMD virus serotypes), from a different species (i.e., isolates from both Pasteurella haemolytica and Pasteurella multocida), or a vaccine containing a combination of antigens from different genera (for example, a vaccine comprising antigens from Pasteurella multocida, Salmonella, Escherichia coli, Haemophilus somnus and Clostridium).
  • Suitable pharmaceutically acceptable carriers include, but are not limited to, sterile water, saline, glucose, dextrose, or buffered solutions. Carriers may include auxiliary agents including, but not limited to, diluents, stabilizers (i.e., sugars and amino acids), preservatives, wetting agents, emulsifying agents, pH buffering agents, viscosity enhancing additives, colors and the like.
  • the term“vaccine composition” includes at least one antigen or immunogen in a pharmaceutically acceptable vehicle useful for inducing an immune response in a host.
  • Vaccine compositions can be administered in dosages and by techniques well known to those skilled in the medical or veterinary arts, taking into consideration such factors as the age, sex, weight, species and condition of the recipient animal, and the route of administration.
  • the route of administration can be percutaneous, via mucosal administration (e.g., oral, nasal, anal, vaginal) or via a parenteral route (intradermal, intramuscular, subcutaneous, intravenous, or intraperitoneal).
  • Vaccine compositions can be administered alone, or can be co-administered or sequentially administered with other treatments or therapies.
  • Forms of administration may include suspensions, syrups or elixirs, and preparations for parenteral, subcutaneous, intradermal, intramuscular or intravenous administration (e.g., injectable administration) such as sterile suspensions or emulsions.
  • Vaccine compositions may be administered as a spray or mixed in food and/or water or delivered in admixture with a suitable carrier, diluent, or excipient such as sterile water, physiological saline, glucose, or the like.
  • compositions can contain auxiliary substances such as wetting or emulsifying agents, pH buffering agents, adjuvants, gelling or viscosity enhancing additives, preservatives, flavoring agents, colors, and the like, depending upon the route of administration and the preparation desired.
  • auxiliary substances such as wetting or emulsifying agents, pH buffering agents, adjuvants, gelling or viscosity enhancing additives, preservatives, flavoring agents, colors, and the like, depending upon the route of administration and the preparation desired.
  • Standard pharmaceutical texts such as“Remington's Pharmaceutical Sciences,” 1990 may be consulted to prepare suitable preparations, without undue experimentation.
  • the immunogen or antigen suitable for use in the present invention may be selected from the group consisting of inactivated pathogens, attenuated pathogens, immunogenic sub-units (e.g. proteins, polypeptides, peptides, epitopes, haptens), or recombinant expression vectors, including plasmids having immunogenic inserts.
  • the immunogen is an inactivated or killed microorganism.
  • the vaccine composition comprises an immunogen selected from the group of avian pathogens including, but not limited to, Salmonella typhimurium, Salmonella enteritidis, Infectious Bronchitis virus (IBV), Newcastle Disease virus (NDV), egg drop syndrome virus (EDS), or Infectious Bursal Disease virus (IBDV), avian influenza virus, and combinations thereof.
  • avian pathogens including, but not limited to, Salmonella typhimurium, Salmonella enteritidis, Infectious Bronchitis virus (IBV), Newcastle Disease virus (NDV), egg drop syndrome virus (EDS), or Infectious Bursal Disease virus (IBDV), avian influenza virus, and combinations thereof.
  • the vaccine composition comprises an immunogen selected from a feline pathogen such as feline herpesvirus (FHV), feline calicivirus (FCV), feline leukemia virus (FeLV), feline immunodeficiency virus (FIV), rabies virus, and combinations thereof.
  • a feline pathogen such as feline herpesvirus (FHV), feline calicivirus (FCV), feline leukemia virus (FeLV), feline immunodeficiency virus (FIV), rabies virus, and combinations thereof.
  • a vaccine composition of the present invention comprises an immunogen selected from a canine pathogen including, but not limited to, rabies virus, canine herpesvirus (CHV), canine parvovirus (CPV), canine coronavirus, Leptospira canicola, Leptospira icterohaemorragiae, Leptospira grippotyphosa, Borrelia burgdorferi, Bordetella bronchiseptica and the like, and combinations thereof.
  • rabies virus canine herpesvirus (CHV), canine parvovirus (CPV)
  • canine coronavirus canine coronavirus
  • Leptospira canicola canine herpesvirus
  • CPV canine parvovirus
  • canine coronavirus canine coronavirus
  • Leptospira canicola canicola
  • Leptospira icterohaemorragiae Leptospira grippotyphosa
  • the composition comprises an immunogen selected from an equine pathogen, such as equine herpesvirus (type 1 or type 4), equine influenza virus, tetanus, west nile virus, and the like or combinations thereof.
  • an equine pathogen such as equine herpesvirus (type 1 or type 4), equine influenza virus, tetanus, west nile virus, and the like or combinations thereof.
  • the composition comprises an immunogen selected from an bovine pathogen, such as foot and mouth disease virus (FMDV), rabies virus, bovine rotavirus, bovine parainfluenza virus type 3 (bPIV-3), bovine coronavirus, bovine viral diarrhea virus (BVDV), bovine respiratory syncytial virus (BRSV), Infectious Bovine Rhinotracheitis virus (IBR), E. coli, P. multocida, P. haemolytica and combinations thereof.
  • an immunogen selected from an bovine pathogen, such as foot and mouth disease virus (FMDV), rabies virus, bovine rotavirus, bovine parainfluenza virus type 3 (bPIV-3), bovine coronavirus, bovine viral diarrhea virus (BVDV), bovine respiratory syncytial virus (BRSV), Infectious Bovine Rhinotracheitis virus (IBR), E. coli, P. multocida, P. haemolytica and combinations thereof.
  • FMDV foot and mouth disease virus
  • the composition comprises a vaccine agent, including immunogens and nucleic acids encoding immunogens, selected from an porcine pathogen such as, but not limited to, swine influenza virus (SIV), porcine circovirus type 2 (PCV- 2), porcine reproductive respiratory syndrome virus (PRRS), pseudorabies virus (PRV), porcine parvovirus (PPV), FMDV, M. hyopneumoniae, Erysipelothrix rhusiopathiae, Pasteurella multocida, Bordetella bronchiseptica, E. coli and the like, and combinations thereof.
  • porcine pathogen such as, but not limited to, swine influenza virus (SIV), porcine circovirus type 2 (PCV- 2), porcine reproductive respiratory syndrome virus (PRRS), pseudorabies virus (PRV), porcine parvovirus (PPV), FMDV, M. hyopneumoniae, Erysipelothrix rhusiopathiae,
  • Vaccine agents comprising viruses, bacteria, fungi and the like may be produced by in vitro culture methods using appropriate culture medium or host cells lines and conventional methods well known to those of ordinary skill in the art.
  • PRRS may be cultured in an appropriate cell line, such as MA-104 cell line (see US Patents 5,587,164; 5,866,401; 5,840,563; 6,251,404).
  • PCV-2 may be cultured using PK-15 cells line (see US 6,391,314); SIV may be cultured on eggs (US 6,048,537); and M. hyopneumoniae may be cultured in an appropriate culture medium (US 5,968,525; US 5,338,543).
  • the pathogen is preferably inactivated after harvesting and, optionally, subjected to clarification by means of a chemical treatment using, for example, formalin or formaldehyde, beta-propiolactone, ethyleneimine, binary ethyleneimine (BEI), and/or a physical treatment (e.g. a heat treatment or sonication).
  • a chemical treatment using, for example, formalin or formaldehyde, beta-propiolactone, ethyleneimine, binary ethyleneimine (BEI), and/or a physical treatment (e.g. a heat treatment or sonication).
  • the PRRS virus may be inactivated by beta-propiolactone treatment (Plana-Duran et al., Vet. Microbiol., 1997, 55: 361- 370) or by BEI treatment (US 5,587,164); inactivation of PCV-2 virus may be accomplished using ethyleneimine treatment or by beta-propiolactone treatment (US Patent Serial No. 6,391,314); swine influenza virus may be inactivated using a detergent like Triton, or with formaldehyde treatment (US 6,048,537); M. hyopneumoniae bacterium may be inactivated by formaldehyde treatment (Ross R. F. supra), by ethyleneimine or BEI treatment.
  • the inactivated pathogen can be concentrated by conventional concentration techniques, in particular by ultrafiltration, and/or purified by conventional purification means, in particular using chromatography techniques including, but not limited to, gel-filtration, ultracentrifugation on a sucrose gradient, or selective precipitations, in particular in the presence PEG.
  • Immunogens useful in vaccine compositions according to the present invention also include expression vectors.
  • Such vectors include, but are not limited to, in vivo recombinant expression vectors such as a polynucleotide vector or a plasmid (EP-A2-1001025; Chaudhuri P, Res. Vet. Sci. 2001, 70: 255-6), virus vectors such as, but not limited to, adenovirus vectors, poxvirus vectors such as fowlpox (US 5,174,993; US 5,505,941; and US 5,766,599) or canarypox vectors (US 5,756,103) or bacterial vectors (E. coli or Salmonella sp.).
  • in vivo recombinant expression vectors such as a polynucleotide vector or a plasmid (EP-A2-1001025; Chaudhuri P, Res. Vet. Sci. 2001, 70: 255-6)
  • virus vectors such as, but not limited to,
  • the present invention also encompasses the formulation of multivalent immunological compositions or combination vaccine compositions.
  • antigens useful in a combination bovine bacterin made according to the present invention include, but are not limited to, Mycoplasma bovis, Pasteurella sp., particularly P. multocida and P. haemolytica, Haemophilus sp., particularly H. somnus, Clostridium sp., Salmonella, Corynebacterium, Streptococcus, Staphylococcus, Moraxella, E. coli and the like.
  • the present invention further provides for methods for inducing an immune response in a host, e.g., an animal, comprising administering to the host an immunological composition or a vaccine composition according to the invention.
  • the immune responses elicited in this manner are notably antibody and/or cellular immune responses, and in particular, a ⁇ -interferon response.
  • the present invention provides for methods to immunize against, or to prevent or to reduce the symptoms caused by, infection of an animal with a pathogenic organism (for example, infection by a virus, bacteria, fungus, or protozoan parasite).
  • the method of the present invention is useful in vertebrate animals including, but not limited to, humans, canines (e.g., dogs), felines (e.g., cats); equines (e.g., horses), bovines (e.g., cattle) and porcine animals (e.g., pigs), as well as in avians including, but not limited to, chickens, turkeys, ducks, geese, a quail, a pheasant, parrots, finches, hawks, crows and ratites (ostrich, emu, cassowary, etc.).
  • canines e.g., dogs
  • felines e.g., cats
  • equines e.g., horses
  • these methods consist of the vaccination of pregnant females before parturition by administering a vaccine composition made according to the invention. These methods further include the induction of protective antibodies elicited by the vaccination protocol and the transfer of these protective antibodies from vaccinated pregnant females to their offspring, to protect the offspring from infection and disease.
  • the dosage of the vaccine composition made according to the present invention will depend on the species, breed, age, size, vaccination history, and health status of the animal to be vaccinated. Other factors like antigen concentration, additional vaccine components, and route of administration (i.e., subcutaneous, intradermal, oral, intramuscular or intravenous administration) will also impact the effective dosage.
  • the dosage of vaccine to administer is easily determinable based on the antigen concentration of the vaccine, the route of administration, and the age and condition of the animal to be vaccinated. Each batch of antigen may be individually calibrated. Alternatively, methodical immunogenicity trials of different dosages, as well as LD 50 studies and other screening procedures can be used to determine effective dosage for a vaccine composition in accordance with the present invention without undue experimentation.
  • the dosage provides at least a partial protective effect against natural infection, as evidenced by a reduction in the mortality and morbidity associated with natural infection.
  • the appropriate volume is likewise easily ascertained by one of ordinary skill in the art.
  • the volume of a dose may be from about 0.1 ml to about 0.5 ml and, advantageously, from about 0.3 ml to about 0.5 ml.
  • the volume of a dose may be from about 0.2 ml to about 3.0 ml, advantageously from about 0.3 ml to about 2.0 ml, and more advantageously, from about 0.5 ml to about 1.0 ml.
  • the volume of dose may be from about 0.2 ml to about 5.0 ml, advantageously from about 0.3 ml to about 3.0 ml, and more advantageously from 0.5 ml to about 2.0 ml.
  • the vaccine composition is administered as a parenteral injection (i.e., subcutaneously, intradermally, or intramuscularly).
  • the composition may be administered as one dose or, in alternate embodiments, administered in repeated doses of from about two to about five doses given at intervals of about two to about six weeks, preferably from about two to about five weeks.
  • the number of doses and the time interval between vaccinations depends on a number of factors including, but not limited to, the age of the animal vaccinated; the condition of the animal; the route of immunization; amount of antigen available per dose; and the like.
  • the period will generally be longer than a week and preferably will be between about two to about five weeks.
  • a booster vaccination before or during pregnancy, at about an annual interval may be performed.
  • the invention further relates to methods to treat a host, e.g., an animal, comprising administering to the host a pharmaceutical composition made according to the invention and comprising at least one immunogen selected from the group consisting of proteins or peptides, inactivated or attenuated virus, antibodies, allergens, CpG ODN, growth factors, cytokines, or antibiotics, and in particular CpG ODN or cytokines.
  • a pharmaceutical composition made according to the invention and comprising at least one immunogen selected from the group consisting of proteins or peptides, inactivated or attenuated virus, antibodies, allergens, CpG ODN, growth factors, cytokines, or antibiotics, and in particular CpG ODN or cytokines.
  • the disclosure provides an immunological or vaccine composition
  • an adjuvant formulation comprising an adjuvant formulation, a therapeutically effective amount of an antigen component, and a pharmaceutically or veterinarily acceptable carrier, wherein the adjuvant formulation comprises a non-crosslinked polyacrylic acid (PAA) polymer having a weight average molecular weight (AMw) of about 350 kDa to about 650 kDa.
  • PAA polyacrylic acid
  • AMw weight average molecular weight
  • the antigen component may comprise an attenuated recombinant viral vector, a naturally or genetically-engineered live attenuated virus or microorganism, an inactivated virus or microorganism, a coccidian microorganism, a precocious coccidian microorganism, a proteinaceous subunit, a single-celled parasite, a multi-cellular parasite or any combination of the preceding.
  • the antigen component may comprise: a canine coronavirus (CCV) antigen, a canine distemper virus (CDV) antigen, a canine parvovirus antigen (CPV), a canine parainfluenza (CPI) antigen, a feline calicivirus (FCV) antigen, a feline immunodeficiency virus (FIV) antigen, a feline herpes virus (FHV) antigen, a feline leukemia virus (FeLV) antigen, a cancer antigen (e.g. Her2-neu, tyrosinase, Il-2 and the like), an Eimeria sp. or antigen thereof, Escherichia coli (E.
  • CCV canine coronavirus
  • CDV canine distemper virus
  • CPV canine parvovirus antigen
  • CPI canine parainfluenza
  • FCV feline calicivirus
  • FV feline immunodeficiency virus
  • FHV feline
  • coli or antigen thereof, Mycoplasma hyopneumoniae (M. hyo), a bovine diarrhea virus (BDV) antigen, a recombinant canarypox vector containing and capable of in vivo expression of at least one protective immunogen, an inactivated full-length rabies glycoprotein, an Erysipelothrix sp., Erysipelothrix rhusiopathiae, a surface protective antigen (SpaA) from E.
  • M. hyo Mycoplasma hyopneumoniae
  • BDV bovine diarrhea virus
  • SpaA surface protective antigen
  • a SpaA fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least
  • the antigen component comprises or consists of an inactivated full- length rabies glycoprotein.
  • the antigen component may also comprise or consist of a C. perfringens B/C toxin, a C. perfringens D toxin, C. septicum toxin, C. novyi toxin, a C. tetani toxin or combinations thereof.
  • the immunological or vaccine composition may comprise an antigen component comprising a C. perfringens B/C toxin, a C. perfringens D toxin, C. septicum toxin, C. novyi toxin and a C. tetani toxin.
  • the PAA adjuvant disclosed herein provides“dose sparing.”
  • the antigen component comprises a SpaA antigen or a fusion protein comprising the SpaA antigen.
  • the antigen component comprises an attenuated avipox virus or a DNA plasmid containing and capable of in vivo expression of an influenza gene.
  • the antigen component may also comprise an attenuated avipox virus or a DNA plasmid containing and capable of in vivo expression of a rabies glycoprotein gene.
  • various methods of treatment are provided.
  • the disclosure provides a method of treating a bovine against infection caused by bacteria comprising administering to the bovine animal vaccine compositions comprising a PAA polymer having a Mw range from about 350 kDa to about 650 kDa.
  • PAA having a Mw of about 450 kDa are exceptionally useful in eliciting in animals, including bovines, protective immune responses.
  • the disclosure provides a method of treating a canine or equine against infection caused by influenza comprising administering to the canine or equine a vaccine comprising an avipox or DNA plasmid containing and capable of in vivo expression of an influenza antigen.
  • the influenza antigen is an HA gene.
  • the disclosure provides a method for treating a canine against infection caused by rabies virus comprising administering to the canine a vaccine composition comprising inactivated rabies glycoprotein and PAA having a Mw from about 350 kDa and 650 kDa.
  • the invention also provides avian vaccines, including an avian coccidiosis vaccine, for in ovo administration, which may comprise:
  • an adjuvant that comprises non-crosslinked PAA having an average Mw from about 350 kDa to about 650 kDa;
  • a protozoan antigen selected from (1) one or more recombinantly expressed proteins; (2) one or more proteins or other macromolecules isolated from said protozoan by conventional means; (3) whole cell extracts or preparations from said protozoan; and (4) inactivated, live or live-precocious coccidians selected from: Eimeria (E.) acervulina, E. adenoeides, E. brunetti, E. colchici, E. curvata, E. dispersa, E. duodenalis, E. fraterculae, E. gallopavonis, E. innocua, E. praecox, E. maxima, E. meleagridis, E. meleagrimitis, E. mitis, E. necatrix, E. phasiani, E. procera, E. tenella and combinations thereof.
  • Eimeria E.
  • acervulina E. adenoeides, E. brunetti, E. col
  • the PAA has an average Mw of about 450 kDa.
  • the invention further provides a method of treating a bovine against infection caused by E. coli or M. hyo comprising administering to the bovine a vaccine composition comprising PAA and E. coli or M. hyo.
  • the invention necessarily encompasses a method of treating a swine against infection caused by M. hyo comprising administering to the swine the vaccine comprising M. hyo.
  • the immunological or vaccine composition comprises an antigen corresponding to an agent responsible for a feline infection and/or disease state.
  • the antigen may comprises feline immunodeficiency virus (FIV).
  • FIV feline immunodeficiency virus
  • the invention also provides a method of treating a feline against infection caused by FIV comprising administering to the feline a vaccine comprising an FIV antigen and PAA.
  • the disclosure provides a vaccine composition comprising a cancer antigen.
  • the disclosure provides a method of treating a subject against cancer comprising administering to the subject the vaccine composition comprising the cancer antigen and PAA.
  • NaPAA designates the polymer sodium salt, whatever it is according to the invention or not.
  • “molecular weight” means“weight average molecular weight”.
  • a Viscotek GPCmax VE2501 system (Malvern Instrument, Malvern, UK) comprising a HPLC pump with built-in degasser and autosampler with 100 ⁇ L injection loop was used to perform the HP-SEC analyses.
  • a Viscotek TDA 302 detector system with refractive index, right angle light scattering and four-capillary differential viscometer detectors was used for on-line SEC signal detection. Detectors were in the following order: LS (right angle light scattering)–RI (refractive index)–VIS (four-capillary differential viscometer).
  • LS right angle light scattering
  • RI reffractive index
  • VIS four-capillary differential viscometer
  • a 0.22 ⁇ m nylon pre-filter was placed between the column and detectors.
  • OmniSEC 4.7 software program was used for the acquisition and analysis of SEC data.
  • Pullulan, DNA and sucrose standards were prepared by dissolution of raw materials in PBS 1C to final concentrations at 1, 0.1 and 2 mg.mL -1 respectively.
  • NaPAA were formulated and diluted at target concentration in PBS 1C.
  • Dn/dc coefficient is related to molar mass according to the following relationship (Zimm, 1948 J chem Phys 16 1099-1116):
  • K is the optical constant which includes dn/dc for a particular scattering system described in following equation
  • C is the concentration of NaPAA in the sample
  • R ⁇ is the excess intensity of light scattered at angle ⁇
  • Mw is the weight-average molecular weight
  • a 2 is the second virial coefficient, which can be taken as zero, owing to the extremely low concentration of the individual sample fractions.
  • P( ⁇ ) is the particle scattering function which represents the angular dependency of light scattering intensity, and is related to radius of gyration (Rg) of the polymer molecule.
  • n 0 being the refractive index of the solvent in the sample
  • N A the Avogadro’s number
  • ⁇ 0 the wavelenght of the laser beam in vacuum.
  • the dn/dc of NaPAA was automaticaly calculated by OmniSEC software using increasing known concentrations of NaPAA with SEC-triple detection system from 0.4 to 1 mg.mL -1 . Each concentration was injected in duplicate. This experiment has been repeated under the same conditions with different representative NaPAA batches of known concentrations. Final dn/dc coefficient corresponded to the mean of these determinations and was determined to be 0.172 mL.g -1 . This dn/dc value was used for further molecular weight determinations.
  • the determinations of Mw, IP and Mark Houwink slope were conducted with a solution of the polyacrylic acid polymer salt in PBS 1C, with a known concentration of the polyacrylic acid polymer salt, for instance of 0.4 mg.mL -1 .
  • the polyacrylic acid salt represents more than 95 % of the dry weight of the polyacrylic acid polymer salt, the weight of the dry matter is considered to be the dry weight of the polyacrylic acid polymer salt.
  • the intrinsic viscosity (IV) of a NaPAA is related to its molecular weight and conformation; and is represented with the Mark-Houwink diagram:
  • a slope "a" superior or equal to 0.7 means that the NaPAA can be considered as linear.
  • Polydispersity Index (IP) is defined as Mw/M n , Mn being the number average molecular weight.
  • Mn of NaPAA was automaticaly calculated by the OmniSEC software.
  • HPAEC High Performance Anion Exchange Chromatography
  • An ICS-3000 (Dionex, Thermo Fisher Scientific, Pittsburgh, PA) ion chromatography system was used. It was equipped with an SP-1 pump, a thermostated autosampler (5°C), thermostated column (40°C) and a conductimetric detector compartment (30°C).
  • An ATC3 RFIC (9x24mm) carbonate trap column (Thermo Fisher Scientific) was positioned in front of the column to capture water carbonate anions and improve global analytical sensitivity.
  • Analytical separation was achieved on an anion exchange AS-11HC column (250x4mm) from Dionex (Thermo Fisher Scientific) with a gradient elution from 25 mM (phase A) to 200 mM (phase B) sodium hydroxide solution.
  • the gradient program was: 0% B (12 min), 0-40% B (5 min), 40-100% B (8 min), 100% B (25 min), 100-0% B (1 min), 0% B (9 min).
  • the flow rate of the mobile phase was 1mL/min and the injection volume was 50 ⁇ L.
  • An AG-11HC pre-column (50x4mm) from Dionex (Thermo Fisher Scientific) was used to protect the analytical column.
  • a Dionex conductivity suppressor (AERS 082540, Thermo Fisher Scientific) was positioned in front of the detector compartment to improve the signal. In these chromatographic conditions, retention times for acrylate, oxalate and persulfate were around 4, 11, and 45 minutes respectively.
  • the quantification of persulfate and acrylate impurities was performed by external calibration prepared with commercial standards. Six concentrations ranging from 1– 100 ⁇ g/mL sodium acrylate and persulfate were mixed in water and 200 ⁇ L of 500 ⁇ g/mL sodium oxalate internal standard was added to each concentration. The calibration curve followed a linear model for persulfate, and a quadratic model for acrylate. The impurities contents were expressed in % w/w (% weight of acrylate or persulfate impurity over dry NaPAA weight) or in ⁇ g of persulfate or acrylate impurity per gram of raw material NaPAA.
  • Persulfate and residual acrylic acid impurities in NaPAA samples after the purification step were determined as described above for their determination in the NaPAA raw material samples. However, in the purified samples, the 10 fold dilution step was omitted from the sample preparation procedure. For persulfate, the chromatographic conditions were the same as for the raw material NaPAA and the analysis was managed as a limit test with a 100 ng/mL limit of detection.
  • acrylate For acrylate, the same HPAEC system was used but the analytical separation was achieved on an anion exchange CarboPacTM SA10 column (250x4mm) from Dionex (Thermo Fisher Scientific) with a gradient elution from 30 mM (phase A) to 200 mM (phase B) sodium hydroxide solution.
  • the gradient program was: 0% B (14 min), 0-100% B (6 min), 100% B (15 min), 100-0% B (1 min), 0% B (9 min).
  • the flow rate of the mobile phase was 1mL/min and injection volume was 50 ⁇ L.
  • a CarboPacTM SA10G column (50x4mm) from Dionex (Thermo Fisher Scientific) was used to protect analytical column.
  • a Dionex conductivity suppressor (AERS 082540, Thermo Fisher Scientific) was positioned in front of detector compartment to improve the signal. In these chromatographic conditions, the retention time for acrylate was around 11 minutes. Residual acrylic acid impurity was determined from a linear calibration curve constructed using an external acrylic acid standard at 20– 500 ng/ml in PBS 1C. Results were expressed as above in % w/w (% weight of acrylate or persulfate impurity over dry NaPAA weight) or in ⁇ g of persulfate or acrylate impurity per mL of NaPAA adjuvant solution.
  • the antigen was prepared in the following manner:
  • Staphylococcus aureus (Reynolds strain) was grown for 72 hours in SATA-1 broth medium under agitation (100 rpm) and then inactivated by the addition of a 1/1 (v/v) phenol/ethanol solution to a final concentration of 2% w/v.
  • Bacteria cells were sedimented at 16 000 g for 75 min.
  • the cell paste was suspended at 0.5 g (wet weight) per ml in 50 mM Tris-2 mM MgSO 4 , pH 7.5. Lysostaphin (100 ⁇ g/ml) was added and the suspension was incubated at 37°C for 4 hours under agitation.
  • benzonase was added at a concentration of 5 U/ml and the incubation was continued for 2 more hours.
  • the reaction mixture was concentrated by tangential flow filtration (30 000 Da molecular-weight cut-off).
  • the resulting concentrated material was digested with benzonase (5 U/ml) for 6 hours at 37°C and then with pronase (at 4 U/ml) at 37°C for 15 hours in the appropriate buffer (Tris 50 mM at pH 8.0 containing 1 mM MgCl 2 and 1 mM CaCl 2 ). After centrifugation at 5000 g for 30 min, the supernatant was concentrated by tangential flow filtration (30000 Da MWCO).
  • the purified polysaccharide was then activated in NaCl by adipic acid dihydrazide (ADH).
  • ADH adipic acid dihydrazide
  • EDAC ethyldimethylaminopropylcarbodiimide
  • the pH was constantly adjusted to a value of 4.9 with 0.1 N HCl.
  • the reaction was stopped by the addition of NaOH up to neutralization (pH 7.0).
  • the activated polysaccharide was then dialyzed against 500 mM NaCl aqueous solution and then against water.
  • the activated and dialyzed polysaccharide was then lyophilized.
  • the percentage functionalization was estimated at about 5.9% (w/w).
  • a solution of the activated polysaccharide was mixed with the carrier protein (rEPA) in NaCl and EDAC.
  • the conjugation took place at 4° C, with a pH maintained at 5.7 through the addition of 0.1 N HCl. After 90 min, the reaction was stopped by addition of 0.2 N NaOH up to a pH of 7.
  • the conjugated antigen was then dialyzed against a NaCl aqueous solution and then purified by size exclusion chromatography on a sepharose Cl-4B column equilibrated with 200 mM NaCl in a 10 mM phosphate buffer, pH 7.2. The fractions which contained conjugates (as detected by optical absorption at 206 nm and 278 nm) and which are mainly eluted with the dead volume of the column, were combined.
  • the polymer formulations were prepared in the following manner:
  • PAA225000 (Ref. 18613, sodium salt) was obtained from Polysciences Europe (Eppelheim, Germany) in the form of a concentrated solution. It has been diluted with water to obtain a concentration of 20 mg/ml, and maintained under agitation at room temperature during 12 hours. The pH has been adjusted to 7.55 with HCl and the solution has been dialyzed at room temperature against 150 mM NaCl aqueous solution (3 consecutive baths) by using 2kDa cutoff dialysis cassettes (Thermo Fischer Scientific, Courtaboeuf, France). The solution was then filtered through a 0.22 ⁇ m PVDF membrane, for sterilization. The Molecular Weight of the polymer salt was then measured and is 488550 Da. Its Mn was 129070 Da and its IP 3.8.
  • the polymer was then stored at + 4°C, as a solution comprising 20mg/ml of polymer in 150 mM NaCl aqueous solution. This solution was then mixed with PBS 1C concentrated 10 times with sterile water, in order to get a saline solution comprising 2mg/ml of polymer salt.
  • Product named PAA20 was obtained as a sodium salt from Polymer Expert (Pessac, France) in the form of a dry powder. It was rehydrated in water to the concentration of 20 mg/ml and maintained under agitation at room temperature during 12 hours. The solution was then filtered through a 0.22 ⁇ m PVDF membrane, for sterilization. The Molecular Weight of the polymer salt was measured at 100 700 Da. Its Mn was 46700 Da and its IP 2.2. The polymer was then stored at + 4°C, as a solution comprising 20mg/ml of polymer salt in 150 mM NaCl aqueous solution.
  • CARBOPOL ® 974 P (named CARBOPOL ® ) which is a reticulated PAA polymer, with a Molecular Weight of several millions Da, was diluted with PBS to get a solution comprising 2mg/ml of polymer.
  • the adjuvanted formulations to be injected to animals were prepared by vol/vol mixing of the antigen solution and of the polymer solution. Each injected dose had 200 ⁇ g of polymer and 2.5 ⁇ g of polysaccharide in PBS 1C solution.
  • mice Groups of 5 to 10 OF1 mice, aged 7 to 9 weeks, were immunized either with PAA20, PAA225000 or CARBOPOL ® alone (these were used as negative controls) or with the formulations comprising both the antigen and the adjuvant.
  • One group of mice was injected with PS5-rEPA alone. Doses were administered via the subcutaneous (SC) route in the scapular region on D0, D21 and D35. Blood samples were collected on D42 for immune response analysis.
  • SC subcutaneous
  • Blood samples were collected in vacutainer tubes containing a coagulation activator and a serum separator gel (Becton Dickinson, Meylan, France). Tubes were centrifuged at 2600g for 20 min to separate serum from cells. Sera were transferred into deep-well plates and heat-inactivated at 56°C for 30 min before storage at–20°C until their use in subsequent assays.
  • a coagulation activator and a serum separator gel (Becton Dickinson, Meylan, France).
  • Tubes were centrifuged at 2600g for 20 min to separate serum from cells.
  • Sera were transferred into deep-well plates and heat-inactivated at 56°C for 30 min before storage at–20°C until their use in subsequent assays.
  • the test comprised different groups as follows:
  • PS5-rEPA + PAA225000 The blood samples were used to test the specific IgG1 and the IgG2a antibodies produced by the immunized mice.
  • the ELISA test used activated polysaccharide PS5 (PS5 conjugated to ADH: PS5-AH) as antigen for the coating. Briefly, ELISA plates were coated with 100 ⁇ L per well of 1 ⁇ g/mL of activated polysaccharide solution in PBS 1C. Plates were incubated 12 hours at 4°C and emptied by plate inverting.
  • hPMNs human peripheral mononuclear cells
  • OPA medium RPMI-Hepes supplemented with 0.5% BSA and 2mM Glutamine
  • bacteria were washed twice in PBS 1C and re-suspended in 5 mL PBS 1C. Bacterium concentration was adjusted to 10 8 CFUs/mL in OPA medium.
  • An oxidative burst assay was performed in a 96-well polypropylene Deepwell plate. The plate was kept on ice upon sequential addition of the reagents. Reagents were added to the wells in the following order: 50 ⁇ L of heat-inactivated specific sera at the determined dilution from 1/10 to 1/640, 250 ⁇ L of bacteria, 50 ⁇ L of baby rabbit complement at 1/10, 100 ⁇ L of leukocytes and 50 ⁇ L of DHR (Molecular Probe, D632) at 1 mg/mL. The final volume of reaction was 500 ⁇ L. The plate was then incubated for 25 min at +37°C under gentle shaking, in the dark.
  • the final bacteria/large leukocyte ratio was 100:1, the final dilution of sera and complement ranged from 1/100 to 1/6400 and the final concentration of the DHR was 0.1 mg/mL.
  • the plate was placed on ice to stop the reaction. Analysis was performed on the Cytomics FC500.
  • the oxidized form of DHR, rhodamine 123 emits a bright fluorescence upon excitation at 488 nm.
  • a gate was defined on the large granular population of leukocytes to differentiate the PMN population. Three thousand events were acquired from each well on this gate. Results were expressed as the percentage of fluorescent activated PMNs (Rhodamine 123-positive PMNs) among the entire PMN population.
  • PS5-rEPA conjugate elicited anti-PS5 serum antibodies able to weakly activate hPMNs in presence of bacteria.
  • the percentage of activated hPMNs producing oxidative burst was estimated at 30% to 70% for a 1/100 serum dilution.
  • the Lowenstein S. aureus strain was cultured 12 hours in TSB medium. Bacterial cells were pelleted, washed with OPA medium (RPMI+5 % SVF+0.05% Tween 20), and suspended in normal saline to 5 x 10 7 cells per mL. The following substances were added into each tube: 0.25 mL PMNs, 50 ⁇ L of diluted test serum, 50 ⁇ L homologous S. aureus cells (ratio 1 cell/1 bacteria), 50 ⁇ L of 0.5% w/v rabbit complement and OPA medium to complete volume at 500 ⁇ L/well. Control tubes with S. aureus in the presence of PMNs, test serum, or complement alone were included in the assay.
  • OPA medium RPMI+5 % SVF+0.05% Tween 20
  • Assay tubes were incubated for 1 hour at +37°C with shaking. Dilutions were performed in 3-steps (3* 1/15 dilutions) and 50 ⁇ L of the different dilutions were dropped six times in TSA gelose and incubated during 12 hours. The percentage of bacterial survival was defined at each dilution point, if possible, using the formula: (number of viable bacterial/original inoculum) x100.
  • PS5-rEPA conjugate elicited anti-PS5 serum antibodies displaying a weak killing activity in presence of hPMNs with a bacterial killing percentage of 39% at 1/100 serum dilution. Bacterial killing activity was not more measured when pool of sera was diluted to 1/500.
  • Co-injection of PS5-rEPA with PAA20 did not improve the ability of anti-PS5 serum antibodies to kill of S. aureus Lowenstein strain.
  • the aim of this study was to evaluate the impact of the Molecular Weight of the polyacrylic acid (PAA) polymer on the adjuvant effect. This has been done by using as a model antigen a recombinant protein which derives from the gB glycoprotein of the human cytomegalovirus (hCMV-gB).
  • PAA polyacrylic acid
  • This recombinant protein was produced by a recombinant CHO line transfected with a plasmid called 0708985pEE14.4, which contains a modified gB gene.
  • the gB gene the sequence of which is described in U.S. Pat. No. 5,834,307, was modified beforehand by deleting the part of the gene which encodes the transmembrane region of the gB protein corresponding to the amino acid sequence between valine 677 and arginine 752 and introducing 3 point mutations at the cleavage site.
  • the protein produced by the CHO line, called gBdTM corresponds to a truncated gB protein depleted of the cleavage site and of the transmembrane region.
  • the gBdTM protein produced in the culture medium was subsequently purified by chromatography and stored in the form of a stock solution containing >0.2 mg/ml of gBdTM in phosphate buffer.
  • the PAA with different molecular weights were as follows: PAA20 and PAA225000 as described and prepared in the paragraph“1) Evaluation of the adjuvant effect of PAA according to the invention in comparison with 2 PAAs of the prior art, in relation with Staphylococcus aureus antigen”.
  • PAA3000 (Ref. 06568), PAA6000 (Ref. 06567), PAA50000 (Ref. 00627) and PAA60000 (Ref. 18611) are NaPAA and were provided by Polysciences in the form of dry powder (for PAA6000) or concentrated solutions for the others.
  • PAA20 was mixed with water to the concentration of 20 mg/ml and maintained under stirring at room temperature during 12 hours. The solution was then filtered through a 0.22 ⁇ m PVDF membrane and kept stored at + 4°C, as a solution comprising 20mg/ml of polymer in 150 mM NaCl aqueous solution. This solution was then mixed with PBS 10C and sterile water, in order to get a saline solution comprising 2mg/ml of polymer.
  • the PAAs from Polysciences were diluted with sterile water to a concentration of 20 mg/ml, adjusted to pH around 7.4 (with the exception of PAA60000 which was not pH adjusted) with NaOH or HCl and dialyzed against 150 mM NaCl (3 consecutive baths) by using a 2kDa cut- off dialysis cassettes (Thermo Fischer Scientific, Courtaboeuf, France). The solutions were then filtered through a 0.22 ⁇ m PVDF membrane, for sterilization. The Mw, Mn and IP were determined and the polymers were stored at + 4°C, as a solution comprising 20mg/ml of polymer salt in 150 mM NaCl aqueous solution. The Molecular weights (Mw and Mn) and PI of the polymers are indicated in the Table 3 below:
  • a squalene emulsion containing the same components as the MF59® squalene emulsion of Novartis was prepared by microfluidisation in order to compare the adjuvant activity of the different polymers to that of prior art adjuvant used as a reference.
  • the adjuvanted formulations were prepared by vol/vol mixing of the antigen solution with the adjuvant solution.
  • the adjuvant quantity was 200 ⁇ g of polymer per injected dose, or in the case of the emulsion, the final vaccine dose comprised 2.5% v/v of squalene.
  • spleens were collected in sterile conditions from 5 mice per group. Splenocytes were isolated as follows: freshly collected spleens were dissociated with Gentlemax dissociator (Miltenyi Biotec), cell suspensions were passed through a cell strainer and washed with RPMI medium. Red blood cells were lysed using Red Blood Cell Lysing Buffer (Sigma). After washing, splenocytes were counted and immediately used for the cellular assays. Seroneutralisation assays:
  • This technique was used to titrate the functional neutralizing antibodies present in the sera of hCMV-gB immunized animals. Based on the ability of the Cytomegalovirus to infect MRC5 fibroblasts and ARPE-19 cells (human epithelial cells), a serum containing specific functional antibodies against HCMV-gB can inhibit the viral infection of the cells.
  • MRC-5 fibroblasts were cultured in 96-well flat bottom plates in DMEM 1% FBS for 1 day in a 5% CO 2 cell culture incubator at 37°C.
  • Heat-inactivated sera from immunized animals were serially diluted with 1% FBS (fetal bovine serum) in DMEM (Dulbecco’s Modified Eagle’s Medium) supplemented with 10% of baby rabbit complement and incubated vol/vol with 3.3 log CCID50 (cell culture infective dose 50%)/ml of hCMV Towne strain for 1 hour in the cell culture incubator.
  • the serum/virus mixtures were then transferred onto the MRC-5 cell monolayers.
  • Neutralizing end-point titers were defined as the reciprocal of the last dilution that fell below the calculated 50% specific-signal value.
  • Neutralizing titers ( ⁇ PRNT50) were defined for each individual serum as the last dilution that induced 50% reduction of infected cells, i.e. the last dilution that induced less cell infection than the calculated 50% specific-signal value.
  • Geometric mean neutralizing antibody titers were calculated for each group.
  • the polyacrylic acid polymer of the present invention gave, by far, the best response. IgG1 and IgG2c antibody responses
  • Serum IgG1 and IgG2c antibodies directed against hCMV-gB antigen were titrated by a robot ELISA assay according to the following procedure.
  • Dynex 96-well microplates were coated during 12 hours at 4°C with 1 ⁇ g / well of hCMV- gB, in 0.05 M carbonate/ bicarbonate buffer, pH 9.6 (Sigma). Plates were then blocked 1 hour at 37°C with 150 ⁇ L/well of PBS Tween-milk (PBS pH7.1, 0.05 % Tween 20, 1% (w/v) powdered skim milk (DIFCO)). All next incubations were carried out in a final volume of 100 ⁇ L, followed by 3 washings with PBS pH 7.1, 0.05 % Tween 20.
  • the reaction was stopped with 100 ⁇ L/well of HCl 1M (Prolabo).
  • Optical density (OD) was measured at 450 nm-650 nm with a plate reader (Spectra Max– Molecular Devices).
  • the IgG antibodies titers were calculated using the CodUnit software, for the OD value range of 0.2 to 3.0 from the titration curve (reference mouse hyper immune serum put on each plate).
  • the IgG titer of this reference expressed in arbitrary ELISA units (EU) corresponded to the log10 of the reciprocal dilution giving an OD of 1.0.
  • the threshold of antibody detection was 10 ELISA units (1.0 log10). All final titers were expressed in log10 (Log).
  • the PAA of the present invention is particularly efficient in increasing the immune response of the T helper1 type (Th1), as the IgG2c titers are particularly strong in mice immunized with hCMV-gB combined with PAA of the present invention.
  • Splenocytes from immunized mice were isolated immediately after sacrifice at day 41, plated at 2.5x10 5 cells per well in 96-well plates and incubated with hCMV-gB (5 ⁇ g/well), concanavalin A (0.25 ⁇ g/well; positive control) or medium alone (RPMI-GSP ⁇ -10% FCS; background). After 6 days of incubation, the secretion of the IL5 and IFN ⁇ cytokines was measured using the CBA Flex set Kit. Results are expressed as cytokine concentrations in pg/ml (geometric mean per group). Threshold for positive cytokine detection was 5 pg/ml for IL-5 and 2.5 pg/ml for IFN ⁇ .
  • the product obtained from Polysciences was simply diluted with PBS and sterile-filtered through a 0.2 ⁇ m cut-off membrane.
  • the concentration of the PAA salt was 17.4 mg/mL.
  • the Mw, IP, and Mark Houwink slope were determined.
  • the obtained solution contained 15.9 mg/mL of the PAA salt with a pH of 7.3.
  • the Mw, IP and Mark Houwink slope were determined.
  • the Molecular weights Mw and the IP of the polymer before and after diafiltration are consistent with the fact that the monomers and the small oligomers, in particular those less than 2000 Daltons have been eliminated by the diafiltration step.
  • immunization formulations were prepared by mixing one of the polymer preparations with the gB solution in the proper ratio, in order to get doses of 50 ⁇ l which each contained 2 ⁇ g of gB and:
  • mice C57BL/6J mice, aged 7 weeks, were immunized twice by the intra-muscular route at Day 0 and Day 21, by one of the prepared formulations. Each preparation was tested in a group of 5 mice. As a control, one group of 5 mice received the antigen alone.
  • the cellular (IFN ⁇ and IL5) and the humoral responses (IgG antibody subclasses, seroneutralizing antibodies) of immunized mice were monitored 2 weeks after the last immunization (on Day 35) in the same way as described in paragraph“2) Testing the adjuvant effect of different polymers on the immune response induced by hCMV-gB”.
  • the adjuvant according to the present invention induced strong Th-1 immune responses accompanied with the induction of strong virus neutralizing antibody titers, and that there was no significant difference between the mice immunized with a diafiltered formulation and the mice immunized with a non-diafiltered formulation.
  • non-diafiltered preparation and diafiltered preparation were used.
  • the purification was carried out by diafiltration with a membrane of a 50 kDa cut off, and the resulting diafiltered preparation contained 8 mg/mL of a PAA polymer salt having a Molecular weight of 443553 Da in PBS 1C.
  • a sodium salt of Polyacrylic Acid Polymer (provided by Polysciences) was sterilized in an autoclave at a temperature of 121°C during 15 minutes.
  • the concentration of the PAA salt in the solution was 101.8 mg/g.
  • the Table 7 hereafter shows the Mw, IV (Intrinsic viscosity) and Mark Houwink slope of the PAA salt after and before autoclaving.
  • Example 3 PAA supports a strong response and decreases antigen payload
  • a new formulation will function as a safe and protective vaccine.
  • Variables that impact whether or not a new formulation will function as a safe and protective vaccine include, but are not limited to: 1) adjuvant type/presence; 2) antigen type/nature (peptide, nucleic acid, killed virus, bacterin, etc.); 3) route of administration; 4) target pathogen type/strain; and 5) target species to be vaccinated. Accordingly, the safety and efficacy of a new vaccine adjuvant must be demonstrated across at least several combinations of these variables before any meaningful conclusions as to its general applicability can be drawn.
  • Example 4 PAA supports a protective response in canine when formulated with classical inactivated or recombinant vaccines
  • *AF03 is an alternative squalene emulsion-based adjuvant, produced using phase inversion (see J. Pharm. Sciences, Vol 101, Issue 12, 2012, and herein incorporated by reference in its entirety).
  • **Squalene emulsion is prepared using high pressure homogenization to form an oil-in-water emulsion Canarypox-vectored influenza study.
  • Canarypox-vectored influenza vaccine formulations were prepared and tested on 5 groups, each containing 7 dogs (Table 12), and the results are presented in FIG. 10. High levels of IFN ⁇ -producing cells were detected in all groups at D14, D27 and D41. Similar to the trend observed for the classical inactivated vaccine formulation above, the canarypox-vectored influenza antigens appear to be better adjuvanted by the higher MW PAA (i.e. PAA225000).
  • vCP2242 is fully described and enabled by US 7,425,336 (to Merial), and herein incorporated by reference in its entirety. But briefly here, vCP2242 is a recombinant ALVAC containing a codon-optimized HA gene from an H3N8 equine influenza virus (EIV), wherein the HA gene is inserted at the ALVAC C5 loci.
  • EIV equine influenza virus
  • PAA is an effective adjuvant for porcine vaccines “SpaA” antigen porcine study.“SpaA” is intended to mean the“surface protective antigen” of Erysipelothrix rhusiopathiae, which is a pathogen that infects porcines and other animals, including canines. Erysipelothrix rhusiopathiae is a Gram-positive, catalase-negative, rod-shaped, non-spore-forming, non-acid-fast, non-motile bacterium. In pigs, E.
  • TS6 means an oil-in-water emulsion described in, for example, US 7,371,395 (to Merial). TS6 is formulated by adding about one (1) part of an antigen-containing aqueous component to about two (2) parts of an oily component, and then emulsifying the two components to form the final emulsion.
  • 150 ⁇ g of SpaA in 2/3 treatment volume (tt) means 100 ⁇ g SpaA by 1/1 volume of tt.
  • the effective amount of SpaA delivered to each Group was 100 ⁇ g. While G1 produced the best results, it is notable that much of the dose volume for oil-in- water emulsions is taken up by the non-antigen components (as above, there is a 2:1 ratio of oily components to aqueous antigen components).
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use as an adjuvant in a vaccine composition, characterized in that said polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 350 to 650 kDa.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to paragraph 1, characterized in that said polyacrylic acid polymer salt is exclusively composed of units corresponding to a salt of acrylic acid or is exclusively composed of units corresponding to the free acid form of acrylic acid and of units corresponding to a salt of acrylic acid.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to paragraph 1 or 2, characterized in that it comprises less than 0.005% w/w of oxidizing agents, based on the total dry weight of said polyacrylic acid polymer salt.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any of the preceding paragraphs, characterized in that it comprises less than 0.001% w/w of oxidizing agents, based on the total dry weight of said polyacrylic acid polymer salt.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one paragraphs 1 to 3, characterized in that it comprises less than 0.005% w/w of persulfates, based on the total dry weight of said polyacrylic acid polymer salt.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any of the preceding paragraphs, characterized in that it comprises less than 0.001% w/w of persulfates, based on the total dry weight of said polyacrylic acid polymer salt.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized in that said polyacrylic acid polymer is a salt with Na+.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized in that said polyacrylic acid polymer salt has a polydispersity index below or equal to 4, preferably below or equal to 2.5.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized in that said polyacrylic acid polymer salt has a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 4; or has a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 4; or has a weight average molecular weight Mw in the range of 380 to 620 kDa and a polydispersity index below or equal to 2.5; or has a weight average molecular weight Mw in the range of 400 to 600 kDa and a polydispersity index below or equal to 2.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized in that said polyacrylic acid polymer salt has a Mark Houwink slope higher or equal to 0.7.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized in that it comprises less than 0.005% w/w of acrylic acid monomer in free acid form or salt form, based on the total dry weight of said polyacrylic acid polymer salt.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized in that it is in a liquid formulation which has a pH in the range of 5.5 to 8.0.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer in salt form for its use according to paragraph 10, characterized in that it is in a buffered aqueous solution, in particular with a phosphate buffer, or a TRIS, Hepes, histidine or citrate buffer.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized in that it is diafiltered.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized in that it is sterilized.
  • a pharmaceutically acceptable salt of a linear or branched polyacrylic acid polymer for its use according to any one of the preceding paragraphs, characterized it is used for enhancing the Th1 immune response obtained with the vaccine composition.
  • a vaccine composition comprising at least one vaccine agent and a pharmaceutically acceptable salt of polyacrylic acid polymer according to anyone of paragraphs 1 to 16, as an adjuvant.
  • the antigen is a bacterial antigen originating from Clostridium tetani, Clostridium diphtheriae, Bordetella pertussis, Haemophilus influenzae type B, Streptococcus pneumoniae, Neisseria meningitidis, Shigella sp, Salmonella typhi, Staphylococcus aureus, Staphylococcus epidermidis, Mycobacterium tuberculosis, Chlamydia trachomatis or pneumoniae or Streptococcus sp; or is a viral antigen originating from the hepatitis A, B or C virus, the influenza virus, the respiratory syncytial virus, the rhinovirus, the West Nile virus, the rabies virus, the poliovirus, the HIV virus, the dengue virus, the Japanese encephalitis virus, the yellow fever virus, the cytomegalovirus or the herpes virus; or is a bacterial antigen originating from Clostridium t
  • the at least one vaccine agent is an antigen or a vector such as a recombinant virus or nucleic acid encoding an antigen, the said antigen being originated from Staphylococcus aureus or from the cytomegalovirus.
  • the vaccine composition according to any one of paragraphs 17 to 21 characterized in that it is in a liquid form having a pH in the range of 6.0 to 8.0.
  • the vaccine composition according to paragraph 21 characterized in that it is in a buffered aqueous solution, in particular with a phosphate buffer or in a TRIS, Hepes, histidine or citrate buffer.
  • the vaccine composition according to any one of paragraphs 17 to 23 for its use in raising an immune response in an individual, in particular in a human being, with enhancement of the obtained Th1 immune response and/or with a balance between the obtained Th1 and Th2 immune responses.
  • a process for the preparation of a pharmaceutically acceptable salt of a polyacrylic acid polymer according to anyone of paragraphs 1 to 16 comprising the following successive steps:
  • a process for the storage of a solution of the polyacrylic acid polymer salt according to anyone of paragraphs 1 to 16 comprising the preparation process according to any one of the paragraphs 25 to 32, followed by a storage step of the obtained pharmaceutically acceptable salt of the polyacrylic acid polymer, in solution.
  • An immunological or vaccine composition comprising a therapeutically effective amount of an antigen component, a pharmaceutically or veterinarily acceptable carrier, and an adjuvant comprising or consisting essentially of a non-crosslinked polyacrylic acid (PAA) polymer having a Mw from about 350 kDa to about 650 kDa and a polydispersity index of less than about 4 or less than about 2.
  • PAA polyacrylic acid
  • composition of paragraph 35, wherein the PAA has a Mw from about 400 kDa to about 600 kDa.
  • composition of paragraph 36, wherein the PAA has a Mw from about 400 kDa to about 500 kDa.
  • the antigen component comprises an attenuated recombinant viral vector, a naturally or genetically-engineered live attenuated virus or microorganism, an inactivated virus or microorganism, a coccidian microorganism, a precocious coccidian microorganism, a proteinaceous subunit, a single-celled parasite, a multi-cellular parasite or any combination of the preceding.
  • the antigen component comprises: an Eimeria sp. or antigen thereof, Escherichia coli (E. coli) or antigen thereof, Mycoplasma hyopneumoniae (M. hyo), a bovine diarrhea virus (BDV) antigen, a recombinant canarypox vector containing and capable of in vivo expression of at least one protective immunogen, an inactivated full-length rabies glycoprotein, an Erysipelothrix sp., Erysipelothrix rhusiopathiae, a surface protective antigen (SpaA) from E.
  • Eimeria sp. or antigen thereof Escherichia coli (E. coli) or antigen thereof, Mycoplasma hyopneumoniae (M. hyo), a bovine diarrhea virus (BDV) antigen
  • BDV bovine diarrhea virus
  • a recombinant canarypox vector containing and
  • a SpaA fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least a portion of at least one additional immunogen
  • a SpaA—FlaB fusion protein comprising at least
  • the antigen component comprises or consists of a C. perfringens B/C toxin, a C. perfringens D toxin, C. septicum toxin, C. novyi toxin, a C. tetani toxin or combinations thereof.
  • the antigen component comprises C. perfringens B/C toxin, a C. perfringens D toxin, C. septicum toxin, C. novyi toxin and a C. tetani toxin.
  • the antigen component comprises an attenuated avipox virus or a DNA plasmid containing and capable of in vivo expression of an influenza gene.
  • the antigen component comprises an attenuated avipox virus or a DNA plasmid containing and capable of in vivo expression of a rabies glycoprotein gene.
  • a method of treating a bovine against infection caused by bacteria comprising administering to the bovine animal the vaccine composition of paragraph 41.
  • a method of treating a canine or equine against infection caused by influenza comprising administering to the canine or equine the vaccine composition of paragraph 44.
  • a method of treating a canine against infection caused by rabies virus comprising administering to the canine the vaccine composition of paragraph 44.
  • An avian coccidiosis vaccine for in ovo administration, which comprises:
  • a protozoan antigen selected from (1) one or more recombinantly expressed proteins; (2) one or more proteins or other macromolecules isolated from said protozoan by conventional means; (3) whole cell extracts or preparations from said protozoan; and (4) inactivated, live or live-precocious coccidians selected from: Eimeria (E.) acervulina, E. adenoeides, E. brunetti, E. colchici, E. curvata, E. dispersa, E. duodenalis, E. fraterculae, E. gallopavonis, E. innocua, E. praecox, E. maxima, E. meleagridis, E. meleagrimitis, E. mitis, E. necatrix, E. phasiani, E. procera, E. tenella and combinations thereof.
  • Eimeria E.
  • acervulina E. adenoeides, E. brunetti, E. col
  • a method of treating a bovine against infection caused by E. coli or M. hyo comprising administering to the bovine the vaccine composition of paragraph 39, wherein the antigen component comprises E. coli or M. hyo.
  • a method of treating a swine against infection caused by M. hyo comprising administering to the swine the vaccine composition of paragraph 51.
  • a method of treating a feline against infection caused by FIV comprising administering to the feline the vaccine composition of paragraph 53.
  • a method of treating a subject against cancer comprising administering to the subject the vaccine composition of paragraph 55.
  • a method of treating a canine against infection caused by CCV comprising administering to the canine the vaccine composition of paragraph 57.
  • a method of treating a bovine against infection caused by bovine rotavirus comprising administering to the bovine the vaccine composition of paragraph 59.
  • a method of treating a canine against infection caused by CIV comprising administering to the canine the vaccine composition of paragraph 61.
  • non-crosslinked polyacrylic acid (PAA) polymer are particularly well-suited for adjuvanting the effect of immunogenic antigens, as well as for eliciting immunological responses independent of the antigens.
  • PAA adjuvants were broadly useful across many different antigen types: an attenuated recombinant viral vector; a classically inactivated rabies glycoprotein; a SpaA peptide subunit; and bacterial toxins.
  • PAA adjuvants functioned well across multiple animal types. Accordingly, Applicants submit that the disclosed non- crosslinked PAAs represent a novel and inventive“universal adjuvant.”

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Abstract

La présente invention concerne de nouvelles formulations immunologiques et vaccinales comprenant un adjuvant polymère d'acide polyacrylique non réticulé nouvellement appliqué. Les adjuvants peuvent être combinés à une grande variété d'immunogènes pour produire des vaccins qui sont sûrs et efficaces lorsqu'ils sont administrés à un large éventail d'animaux cibles. Les immunogènes peuvent comprendre, mais sans s'y limiter : des agents pathogènes inactivés, des agents pathogènes atténués, des sous-unités, des vecteurs d'expression recombinés, des plasmides ou des combinaisons de ces derniers. Les animaux peuvent comprendre, mais sans s'y limiter : des humains, des souris, des chiens, des félins, des équidés, des porcins, des ovins, des caprins et des bovins.
EP17736804.0A 2016-06-17 2017-06-15 Nouvelles formulations immunogènes comprenant des adjuvants polymères d'acide polyacrylique linéaires ou ramifiés Pending EP3471760A1 (fr)

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CA3027877A1 (fr) 2017-12-21
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AU2017286727A1 (en) 2019-01-31
AU2017286727B2 (en) 2024-02-08
US20170360923A1 (en) 2017-12-21
KR20190044052A (ko) 2019-04-29
CN109475615B (zh) 2023-04-07
US11554170B2 (en) 2023-01-17
MX2018015787A (es) 2019-04-22
CN109475615A (zh) 2019-03-15
JP7018941B2 (ja) 2022-02-14
JP2019524873A (ja) 2019-09-05

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